ST. Jude Medical Inc., Crmd
FDA adverse event reports naming ST. Jude Medical Inc., Crmd as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ST. JUDE MEDICAL INC., CRMD.
- Total reports
- 2,954
- Deaths
- 22
- Injuries
- 1,114
- Malfunctions
- 1,806
Reports per year
298
699
304
1506
107
2,92714
Source: FDA adverse event reports by year received, 1998–2014. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Implantable Cardioverter Defibrillator (Non-Crt)LWS1,486
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK770
- Permanent Defibrillator ElectrodesNVY578
- Implantable Pacemaker Pulse-GeneratorDXY62
- Permanent Pacemaker ElectrodeDTB22
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN12
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP10
- Recorder, Event, Implantable Cardiac, (Without Arrhythmia Detection)MXC9
- Pulse Generator, Permanent, ImplantableNVZ2
- Drug Eluting Permanent Left Ventricular (Lv) Pacemaker ElectrodeOJX2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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